norvir patient assistance

could anyone give me ideas as to where or who i would contact to get some patient assistance for acute hep c treatment? I am not working, cannot wait on s.s. disability. I try to do some construction work when available, but it is really rough.

What is your doctor thinking? Is this an HIV Specialist? Are you multi drug resistant? You say your combo is Combivir : which is AZT and 3TC Truvada : which is Viread and Emtriva (which is almost identical to 3TC and should not be taken together) Viread : which is already in the Truvada! Prezista : which is a PI that MUST be taken with Norvir which you aren't on!

The only side effects ill have in the soft stool from time to time, the tingling feeling in my hands and feet from the norvir this too is from time to time, they say the norvir also has gastro effects, I know when it will kill someone....lol.... As of last month my t-cells were 945. I have been positive for 5 years on meds for 4years...

I am a RN and I was giving a patient a SQ insulin shot in the back of her arm, she went to get up as i was finished and the needle went into my left thumb. My heart sank and so did my life. I knew she was HIV+ so i was freaking out right away. As soon as it happened i bled the site and washed it with soap and alcohol. I started PEP 2 hrs later (truvada, norvir, raltegravir, and preszita), my initial results are negative.

Initial counts were 423 viral load (not thousands - just 423) but T cell was 398. Immediately went undetectable. Put on Fortavase, Combivir, Norvir. Soon switched to just Fortavase 8 bid, combivir 1 bid. over time decreased to just 1 fortavase bid and 1 combivir bid. Been up in 700 - 900 T cell the whole time. No one can explain to me why numbers were odd to begin with. Also now that fortavase is off market my doc wants to switch me to Invirase, Combivir and Norvir.

I was reading the post about suboxone prices ,someone wanted to know if the was any assistance for the cost . I did some research this is what I found RECKITT BENCKISER suboxone patient assistance programs 1-866-512-2216 I don't know what are the guidelines but its worth a call . Any little bit I am sure would be very helpful. If I find anything else I will post it.

I wanted to share some encouraging news for people who have Chronic Hep B and have financial difficulty affording Baraclude. I contacted Brystol Myers Squibb and applied for the Patient Assistance Program. The website and application is here: http://www.bms.com/products/Pages/programs.aspx It took about a week and they have approved me to receive the medication and are shipping it to my home.

This is my understanding of the patient assistance programs for Incivek. The list price, which no patient will have to end up paying, is $49,200 for 12 weeks. HOWEVER, the patient assistance programs, are more than generous. Typical Co-pay for the three prescriptions that will be needed will be between $50 and $250 each.

Would your local mental health service have access to that information? Maybe whereever you go for governement assistance (financially) they may have some info. Have you tried a google search?

I started taking PEP on august 4th. I take truvada norvir and reyataz. I went to get a rapid antibody hiv test today and was negative. Should I still be worried and stressed? I haven't slept much since this happened.

Without the patient assistance program I probably wouldn't be SVR - when my insurance refused to let me extend, they coudln't have made it easier and didn't even make me feel bad about needing them to help.

I am also on Copaxone - can I suggest that you talk with them again at Shared Solutions and ask what criteria they use for patient assistance? They fund for people without insurance or underinsured through NORD - national organization of rare disease. Unfortunately it sometimes takes more than one phone call to connect with the right people at SS to get help. If you can't work it out with SS you might talk to your neurologist about other options.

If in need, call the Schering-Plough Patient Assistance Program at 1-800-521-7157 and/or the Roche Patient Assistance Program at 1-877-757-6243. November 10, 2008 http://www.hepatitis-central.com/mt/archives/2008/11/choosing_and_af.

I recently started the Norvir, Reyataz, Truvada combo. This is my first time taking "the meds" after being hiv + for 20 years. I have been on them for only 11 days. I have weird side effects: headaches, queasy stomach, and fatigue/weakness. I told my doctor, and he said, to "tough it out for another week, and he'll see if he needs to change the combination, or switch meds.

There are so many drug assistance programs out there for us in the US who are not on medicare/medicaid or live in Massachussetts. I'm thinking it might be helpful to start a thread of some of these so everyone is taking full advantage of the drug companies' generosity. Ok, you know I'm being facetious with that comment - they want us to take their drug and are bribing us to do so by helping with the copay.

If you go on tysabri, or any other drugs, be sure and get on their patient assistance program. It is great help with the co-pays.

Norvir patient assistance

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